About the job
This job is about supporting clinical research in Medical Oncology at Epworth HealthCare, ensuring it is conducted safely, ethically, and in compliance with Good Clinical Practice (GCP) and regulatory requirements. By assisting with administrative tasks and managing biological specimens, you will play a vital role in enhancing high-quality patient care. The team values collaboration and inclusivity, creating an environment where everyone feels they belong and can contribute to making a difference.
You'll be responsible for
✅
Ensuring compliance with ICH-GCP and TGA guidelines
You will ensure that all research activities adhere to ICH-GCP, TGA guidelines, and ethical standards, maintaining the integrity of the research process.📅
Supporting trial-related activities
You will assist in organizing and coordinating all trial-related activities, including participant visits, in accordance with approved study protocols.📂
Maintaining accurate research documentation
You will be responsible for keeping research study files, clinical documentation, and data up-to-date in both hard copy and within the clinical trials management system (CTMS).Key criteria
🎓
Relevant tertiary qualification
Possession of a degree in science, health care, or related field.View
🔬
Clinical research experience
Demonstrated experience in conducting clinical research activities.View
💻
Computer literacy
Proven ability to effectively use various software and systems.View
View more
